{{Rsnum
|rsid=10509328
|Chromosome=10
|position=72767409
|Orientation=plus
|GMAF=0.1157
|Assembly=GRCh37.p10
|GenomeBuild=37.5
|dbSNPBuild=138
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}
{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 0.0 | 19.5 | 80.5
| HCB | 4.4 | 26.3 | 69.3
| JPT | 2.7 | 29.2 | 68.1
| YRI | 2.0 | 33.3 | 64.6
| ASW | 0.0 | 26.3 | 73.7
| CHB | 4.4 | 26.3 | 69.3
| CHD | 0.9 | 36.7 | 62.4
| GIH | 1.0 | 3.0 | 96.0
| LWK | 0.9 | 13.6 | 85.5
| MEX | 0.0 | 12.1 | 87.9
| MKK | 0.6 | 11.5 | 87.8
| TSI | 1.0 | 18.6 | 80.4
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23502783
  |Trait=Multiple myeloma (IgH translocation)
  |Title=The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma.
  |RiskAllele=G
  |Pval=1E-6
  |OR=1.86
  |ORtxt=[1.45-2.39]
  }}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}